Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

E G Murphy

Showing results (1-10 of 28) with videos related to

Pageof 3
Sort By:
Pediatric Neuroscience|January 1, 1987
Subsarcolemmal vermiform deposits in skeletal muscle, associated with familial cardiomyopathy: report of two cases of a new entityA Calderon, L E Becker, E G Murphy
Pediatric Neuroscience|January 1, 1988
Neurogenic arthrogryposis multiplex congenita: clinical and muscle biopsy findingsC Adams, L E Becker, E G Murphy
Pediatric Neuroscience|January 1, 1988
Heterogeneity of nemaline myopathy. A follow-up study of 13 casesE Shahar, R C Tervo, E G Murphy
Developmental Medicine and Child Neurology|June 1, 1983
Thin ribs on chest X-ray: a useful sign in the differential diagnosis of the floppy newbornJ P Osborne, E G Murphy, A Hill
Journal of Child Neurology|July 1, 1990
Thymectomy in juvenile myasthenia gravisC Adams, D Theodorescu, E G Murphy, et al.
The Journal of Pediatrics|May 1, 1982
Congenital muscular dystrophy: a clinicopathologic report of 24 casesJ B McMenamin, L E Becker, E G Murphy
Canadian Medical Association Journal|May 5, 1973
Nerve conduction in childhood diabetesJ Marcus, R Ehrlich, M Kelly, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1981
Clinical progression of giant-axonal neuropathy over a twelve year periodJ M Dooley, Y Oshima, L E Becker, et al.
Pediatric Neurology|January 1, 1995
Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisoneI Tein, E J Donner, D E Hale, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1993
Familial desminopathy: myopathy with accumulation of desmin-type intermediate filamentsJ Vajsar, L E Becker, R M Freedom, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Pediatric Neuroscience|January 1, 1987
Subsarcolemmal vermiform deposits in skeletal muscle, associated with familial cardiomyopathy: report of two cases of a new entityA Calderon, L E Becker, E G Murphy
Pediatric Neuroscience|January 1, 1988
Neurogenic arthrogryposis multiplex congenita: clinical and muscle biopsy findingsC Adams, L E Becker, E G Murphy
Pediatric Neuroscience|January 1, 1988
Heterogeneity of nemaline myopathy. A follow-up study of 13 casesE Shahar, R C Tervo, E G Murphy
Developmental Medicine and Child Neurology|June 1, 1983
Thin ribs on chest X-ray: a useful sign in the differential diagnosis of the floppy newbornJ P Osborne, E G Murphy, A Hill
Journal of Child Neurology|July 1, 1990
Thymectomy in juvenile myasthenia gravisC Adams, D Theodorescu, E G Murphy, et al.
The Journal of Pediatrics|May 1, 1982
Congenital muscular dystrophy: a clinicopathologic report of 24 casesJ B McMenamin, L E Becker, E G Murphy
Canadian Medical Association Journal|May 5, 1973
Nerve conduction in childhood diabetesJ Marcus, R Ehrlich, M Kelly, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1981
Clinical progression of giant-axonal neuropathy over a twelve year periodJ M Dooley, Y Oshima, L E Becker, et al.
Pediatric Neurology|January 1, 1995
Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisoneI Tein, E J Donner, D E Hale, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1993
Familial desminopathy: myopathy with accumulation of desmin-type intermediate filamentsJ Vajsar, L E Becker, R M Freedom, et al.
Pageof 3